Do you need help implementing your trial protocol but can't afford another full-time employee? Our CRSP team comprises trained, certified, and experienced research nurses, non-nurse coordinators, and regulatory and data personnel who can help fill in the gaps on your research team. You pay only for the amount of effort required. Access a list of CRSP fees here (BlazerID required).
Outsource for Success
We provide the following implementation services in clinical trial and human subject studies:
- Clinical Research Nurse Coordinator (study coordination)
- Clinical Research Coordinator (study coordination)
- Skilled nursing services without study coordination (phlebotomy, IV catheter placement, injections, specimen collection, point-of-care testing)
- Simple specimen processing and shipping
- Specimen transport
- Clinical Research Regulatory Coordinator
- Data management services (Also see our Research Commons domain for data management support)
- ClinicalTrials.gov consultation
- IND/IDE consultation
- Quality Management
- Monitoring
- Study budget development (industry studies)
- Sponsor invoicing (industry studies)
- Study start-up consultation
- Feasibility Assessment and/or Pre-site Selection Questionnaire
- CRSP Recruitment and Retention Consultation
- Pre-site Selection Visit
- Education
CRSP also offers a Clinical Trials Kiosk of helpful implementation tools, including logs, checklists, and standard operating procedures.
Register
To register for a CRSP service, please complete the CBR-CCTS-OCS Submission Form.
CCTS Research Commons offers additional support for study implementation, including access to clinical data, bioethics consultations, and unique CCTS Partner Network resources. Don't see what you need? Have an urgent request? Contact us at